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NCT05316922: WIN-HYPO2021

TSH Suppression During Radiotherapy on Thyroid Site to Prevent Iatrogenic Hypothyroidism in Pediatric Cancer Patients

Recruiting now Phase 3 Last updated 6 December 2023
What this trial tests

Phase 3 trial testing Levothyroxine in Hypothyroidism; Irradiation in 68 participants. Currently enrolling.

Timeline
13 December 2021
Primary endpoint
30 September 2029
30 September 2029

Quick facts

Lead sponsorFondazione IRCCS Istituto Nazionale dei Tumori, Milano
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment68
Start date13 December 2021
Primary completion30 September 2029
Estimated completion30 September 2029
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Fondazione IRCCS Istituto Nazionale dei Tumori, Milano — full company profile →

Who can join

Eligibility, any sex, with Hypothyroidism; Irradiation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To offer the possibility of a treatment that could achieve a meaningful reduction in the incidence of post-radiation therapy hypothyroidism. Thyroid dysfunction may develop from a few months to several years after patients have completed their radiation treatment. In children with chronic diseases, or given lengthy anti-neoplastic treatments, recurrent or persistent endocrine disorders may have a negative effect on growth and development into adulthood.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Levothyroxine

Trials testing the same drug.

Other Fondazione IRCCS Istituto Nazionale dei Tumori, Milano trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05316922.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing